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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
02/03 to 17/03/2021
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2021

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes (incl. QA statement)
Test type:
acute toxic class method

Test material

Constituent 1
Chemical structure
Reference substance name:
1-Methyl-1-propylpyrrolidinium Bis(fluorosulfonyl)imide
EC Number:
922-377-9
Cas Number:
852620-97-4
Molecular formula:
C8H18F2N2O4S2
IUPAC Name:
1-Methyl-1-propylpyrrolidinium Bis(fluorosulfonyl)imide
Test material form:
liquid

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
DMSO
Doses:
300- 2000mg/kg bw/day
No. of animals per sex per dose:
6 at the dose of 300mg/kg bw/day
3 at the dose of 2000mg/kg bw/day

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
> 300 - < 2 000 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
In conclusion, the LD50 of the test item N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide is higher than 300mg/kg bw/day and lower than 2000mg/kg bw/day by oral route in the rat. In accordance with OCDE Guideline 423, the LD50 cut-off of the test item may be considered as 500mg/kg bw/day by oral route in the rat. According to the criteria for classification, packaging and labelling of dangerous substances and preparations in accordance with the Regulation EC No 1272/2008, the test item has to be classified in category 4. The signal word "Warning" and hazard statement H302 "Harmful if swallowed" are required.
Executive summary:

In conclusion, the LD50 of the test item N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide is higher than 300mg/kg bw/day and lower than 2000mg/kg bw/day by oral route in the rat. In accordance with OCDE Guideline 423, the LD50 cut-off of the test item may be considered as 500mg/kg bw/day by oral route in the rat. According to the criteria for classification, packaging and labelling of dangerous substances and preparations in accordance with the Regulation EC No 1272/2008, the test item has to be classified in category 4. The signal word "Warning" and hazard statement H302 "Harmful if swallowed" are required.